Rifa Pharma
Clinical Trial Registration
The need for registration of clinical trials was realized by the govt. and therefore registration has been made mandatory by the Drugs Controller General (India) (DCGI) in CTRI. Multi-country trials, where India is a participating country, which have been registered in an international registry, are also expected to be registered in the CTRI. In the CTRI, details of Indian investigators, trial sites, Indian target sample size and date of enrollment are captured.

After a trial is registered, trials are expected to regularly update the trial status or other aspects as the case may be. After a trial is registered, all updates and changes will be recorded and available for public display.

We  RIFA Pharma providing necessary permissions for conducting clinical trials and in facilitating clinical trials.

 

 


We also provide services for
  • Blood Bank and Blood Product Registration
  • NOC for Import of Half finished or Raw materials
  • Loan Licensing
  • Legalization of Export/Import documents
  • Neutral Code Licensing